warnings
WARNINGS FOR EXTERNAL USE ONLY.
BIO-ICE
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- BIO-ICE
- Generic name
- MENTHOL, CAMPHOR
- Manufacturer
- Electrostim Medical Services Inc. d/b/a EMSI
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1bfd1468-9139-43b1-9709-d47b63d17cfb
- SPL ID
- 463d9205-8ccc-8c5c-e063-6394a90a47c5
- Version
- 8
- Effective date
- 2025-12-18
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:19
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M017 | openfda.application_number | |
| brand name | BIO-ICE | openfda.brand_name | |
| generic name | MENTHOL, CAMPHOR | openfda.generic_name | |
| manufacturer name | Electrostim Medical Services Inc. d/b/a EMSI | openfda.manufacturer_name | |
| ndc | package | 50130-316-11 | openfda.package_ndc |
| ndc | product | 50130-316 | openfda.product_ndc |
| ndc11 | package | 50130031611 | derived:openfda.package_ndc |
| rxcui | 1372902 | openfda.rxcui | |
| spl id | 463d9205-8ccc-8c5c-e063-6394a90a47c5 | id | |
| spl set id | 1bfd1468-9139-43b1-9709-d47b63d17cfb | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.